HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036256Generated: October 26, 2026
Diiodomethane → 4-(5-Fluoro-4-iodo-2-methylphenyl)-2-methylpyridine
https://huagongshe.com/reaction/1036256
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diiodomethane | HCID 6346 | — |
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | 2-Fluoro-5-methyl-4-(2-methylpyridin-4-yl)aniline | HCID 58447709 | — |
| Product | 4-(5-Fluoro-4-iodo-2-methylphenyl)-2-methylpyridine | HCID 58447915 | — |
Reaction Steps
To the solution of 2-fluoro-5-methyl-4-(2-methylpyridin-4-yl)aniline 191-3 (1.02 g, 4.7 mmol) in CH2I2 (16 mL) was added isoamyl nitrite (6 mL) slowly at −10° C. After 20 minutes, the reaction was heated to 100° C. for 2 hours. The solvent was removed by rotary evaporation and the residue was dissolved in ethyl acetate and washed with Na2S2O5, brine and taken to dryness by rotary evaporation. The residue was purified by silica gel flash chromatography, eluted with 40% ethyl acetate in hexane to give 4-(5-fluoro-4-iodo-2-methylphenyl)-2-methylpyridine 191-4. MS m/z 328.10 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546396B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-56d2f48eed5e4bf180414012be71f931 |
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| Source note | uspto-grants-2013_10 |
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